Author

Motee Ashhab

2 papers indexed here

We haven’t gathered this author’s papers yet. Follow them and we’ll fetch their work.

Not the right person? Other researchers publish under this name.

Review Open access Sep 2026

Recurrent homozygous GLRB p.Arg472Ter variant in Palestinian hereditary hyperekplexia: a retrospective genotype–phenotype case series of nine children

Hereditary hyperekplexia is a treatable neurogenetic disorder of impaired glycinergic inhibition that may present neonatally with exaggerated startle, generalized stiffness, and life-threatening tonic apneic spells. Data from Palestine remain limited. We aimed to describe the clinical spectrum, molecular findings...

Samir A. Nasser, O. Salah, Majd Shehadeh et al. · BMC Medical Genomics · 0 citations

Open access Jan 2026

MOG Antibody‐Associated Disease With Bilateral Deep Gray Matter Involvement in a Child: Unique MRI Findings and Therapeutic Response

Myelin oligodendrocyte glycoprotein antibody‐associated disease is an autoimmune inflammatory demyelinating disorder of the central nervous system with diverse clinical and radiological manifestations; however, bilateral symmetric deep gray matter involvement is an exceptionally uncommon presentation in children. We re...

A. Saymeh, H. Abdul-Hafez, Alaa Zayed et al. · Case Reports in Pediatrics · 0 citations